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EC number: 932-185-7 | CAS number: 1187742-72-8
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data
Short-term toxicity to aquatic invertebrates
Administrative data
Link to relevant study record(s)
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 27 SEP - 29 SEP 1994
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.2 (Acute Toxicity for Daphnia)
- GLP compliance:
- yes
- Analytical monitoring:
- yes
- Details on sampling:
- - Concentrations: stock solution and all test concentrations at 0 and 48 h.
- Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
- Method: A stock solution was prepared by adding 1.05 g test substance to 1 L deionised water. The stock solution was diluted with dionised water to give the respective test concentrations. - Test organisms (species):
- Daphnia magna
- Details on test organisms:
- TEST ORGANISM
- Common name: water flea
- Strain: clone 5
- Source: in-house culture
- Age at study initiation: < 24 h
- Method of breeding: for breeding, females are maintained in M4 medium in 1 L beakers. Fedd daily with Scenedesmus subspicatus.
- Feeding during test: none
ACCLIMATION
- Acclimation conditions (same as test or not): M4 medium in 1 L beakers
- Type and amount of food: the amount of food, comprising Scenedesmus subspicatus, is such that the amount added is consumed by the animals.
- Feeding frequency: daily - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 48 h
- Test temperature:
- 20 +/- 1 °C
- pH:
- 7.7 - 7.8
- Dissolved oxygen:
- 7.9 - 8.1 mg/L
- Nominal and measured concentrations:
- Nominal test concentrations: 0.4, 0.7, 1.2, 2.0, 3.5, 6.0 and 10 mg/L
- Details on test conditions:
- TEST SYSTEM
- Test vessel:
- Material, size: round-bottomed test tubes calibrated to 10 mL
- Aeration: none
- No. of organisms per vessel: 5 (+/-1)
- No. of vessels per concentration (replicates): 4
- No. of vessels per control (replicates): 4
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: synthetic fresh water: 294 mg/L CaCl2 x 2H2O, 123 mg/L MgSO4 x 7 H2O, 63 mg/L NaHCO3, 5.5 mg/L KCl
- Ca/Mg ratio: 4 : 1 (2.5 mmol)
OTHER TEST CONDITIONS
- Photoperiod: continous darkness - Reference substance (positive control):
- yes
- Remarks:
- Potassium dichromate
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- 7.7 mg/L
- 95% CI:
- >= 6 - <= 10
- Nominal / measured:
- nominal
- Conc. based on:
- act. ingr.
- Basis for effect:
- mobility
- Results with reference substance (positive control):
- Limit values afer 24 h: 1 mg/L 45% immobilised; 2 mg/L 100% immobilised
- Validity criteria fulfilled:
- yes
- Remarks:
- Please refer to table 3 in "Any other information on results incl. tables"
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study with acceptable restrictions
- Remarks:
- (e.g. non-GLP study; no analytical verification of the test concentrations)
- Principles of method if other than guideline:
- Method: other: Directive 79/831/EEC, Annex V, Part C
- GLP compliance:
- no
- Analytical monitoring:
- no
- Details on test solutions:
- Dilution water chemistry: according to guideline test water specifications
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- Daphnia magna Straus was originally supplied from "Institut National de Recherche Chimique appliquee, France", and has been bred from 1978 in the Laboratories of BASF.
Age: 6 - 24 hours old - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 48 h
- Hardness:
- 2.7 ± 0.5 mmol/L
- Test temperature:
- 292 - 294 K
- pH:
- 8.02 to 10.30
- Dissolved oxygen:
- 8.22 to 10.16 mg/l
- Conductivity:
- 550 - 650 µSiemens/cm
- Nominal and measured concentrations:
- Nominal test concentrations: 500, 250, 125, 62.5, 31.2, 15.6, 7.8, 3.9 and 0 mg/L (control).
- Details on test conditions:
- Exposure vessels: Reagent tubes with flat bottom, 10 ml test volume
Light conditions: Diffuse light
Number of Replicates: Four Individuals /replicate: Five
Preparation of stock solution: Concentration of the substance in the stock solution was 500 mg/L.
Measurements:
a) pH values and dissolved oxygen: After 0 and 48 hours
b) Mobile daphnids: after 0, 3, 6, 24 and 48 hours - Reference substance (positive control):
- not specified
- Duration:
- 48 h
- Dose descriptor:
- EC0
- Effect conc.:
- 62.5 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Remarks:
- not neutralized
- Key result
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- 108.82 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Remarks:
- not neutralized
- Duration:
- 48 h
- Dose descriptor:
- EC100
- Effect conc.:
- 250 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Remarks:
- not neutralized
- Reported statistics and error estimates:
- The method of Spearman Kaerber was used to calculate EC 50 values after 6, 24 and 48 hours of exposure
Referenceopen allclose all
Table 1: Immobilisation after 24 and 48 h.
Concentration |
Test period (h) |
|
24 h |
48 h |
|
Immobility [%] |
Immobility [%] |
|
Control |
5 |
5 |
0.4 |
0 |
0 |
0.7* |
5 |
30 |
1.2 |
5 |
0 |
2.0 |
0 |
0 |
3.5 |
0 |
5 |
6.0 |
0 |
0 |
10 |
40 |
100 |
*not used for evaluation, because no effect could be
observed in case the next following concentration
Table 2: Analytically determined test concentrations
Nominal concentration |
0 h |
48 h |
Concentration for biological valuation [mg/L] |
Control |
0.07 |
-- |
|
0.4 |
0.37 |
0.38 |
0.4 |
0.7 |
0.73 |
0.70 |
0.7 |
1.2 |
1.2 |
1.2 |
1.2 |
2.0 |
1.9 |
2.0 |
2.0 |
3.5 |
3.2 |
3.4 |
3.5 |
6.0 |
5.5 |
5.9 |
6.0 |
10 |
9.1 |
9.7 |
10 |
Stock solution |
955 |
-- |
1000 |
Table 3: Validity criteria for OECD 202 (2004)
Criterion from the guideline |
Outcome |
Validity criterion met |
In the control, including the control containing the solubilising agent, not more than 10% of the daphnids should have been immobilized. |
5% |
yes |
The dissolved oxygen concentration at the end of the test should be ≥ 3 mg/L in control and test vessels. |
7.9 - 8.1 mg/L |
yes |
Mobile daphnids
Nominal conc.(mg/l) |
Mobile daphnids after |
||||
0 h |
3 h |
6 h |
24 h |
48 h |
|
0 |
20 |
20 |
20 |
20 |
20 |
3.9 |
20 |
20 |
20 |
20 |
20 |
7.8 |
20 |
20 |
20 |
20 |
20 |
15.6 |
20 |
20 |
20 |
20 |
20 |
31.2 |
20 |
20 |
20 |
20 |
20 |
62.5 |
20 |
20 |
20 |
20 |
20 |
125 |
20 |
20 |
20 |
20 |
6 |
250 |
20 |
20 |
20 |
0 |
0 |
500 |
20 |
1 |
0 |
0 |
0 |
pH values
Nominal conc.(mg/l) |
pH values after |
|
0 h |
48 h |
|
0 |
8.03 |
8.15 |
3.99 |
8.32 |
8.03 |
7.81 |
8.54 |
8.02 |
15.6 |
8.89 |
8.05 |
31.2 |
9.20 |
8.14 |
62.5 |
9.53 |
8.4 |
125 |
9.79 |
8.71 |
250 |
10.04 |
8.96 |
500 |
10.3 |
9.09 |
Description of key information
EC50 (48 h): 7.7 mga.i./L (nominal, OECD 202)
Key value for chemical safety assessment
Additional information
One GLP-study investigating the short-term toxicity of Alcohols, C12-14 (even numbered), ethoxylated (<=2.5 moles EO), sulfated, monoisopropanolamine salt to aquatic invertebrates is available. The study conducted according to OECD 202 (GLP) in a static system. The test organisms (Daphnia magna) were exposed to nominal substance concentrations of 0.4, 0.7, 1.2, 2.0, 3.5, 6.0 and 10 mg/L. The test concentrations were analytically verified using the MBAS assay (methylene blue active substances assay). The determined recovery rates were > 80%.
. After 48 h an EC50 value of 7.7 mg a.i./L (nominal) was determined.
A study available for monoisopropanolamine (MIPA) determined an EC50 (48 h) of 108.82 mg/L (nominal). The study was conducted according to Directive 79/831/EEC, Annex V, Part C without neutralisation of the test solutions.
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